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ChemistryOpen ; 11(10): e202200169, 2022 10.
Artigo em Inglês | MEDLINE | ID: mdl-36200514

RESUMO

A series of novel heterocyclic structures, namely 1,3-oxazines, 1,3-thiazines and 2,4-diaminopyrimidines, were designed and synthesised. The bioassay tests demonstrated that, among these analogues, 2,4-diaminopyridine derivatives showed significant antiproliferative activity against different human cancer cell lines (A2780, SiHa, HeLa, MCF-7 and MDA-MB-231). Pyrimidines substituted with N2 -(p-trifluoromethyl)aniline, in particular, displayed a potent inhibitory effect on the growth of cancer cells. Structure-activity relationships were also studied from the aspects of stereochemistry on the aminodiol moiety as well as exploring the effects of substituents on the pyrimidine scaffold.


Assuntos
Neoplasias Ovarianas , Tiazinas , Compostos de Anilina/farmacologia , Linhagem Celular Tumoral , Proliferação de Células , Monoterpenos Cicloexânicos , Feminino , Humanos , Oxazinas/farmacologia , Pirimidinas/química , Pirimidinas/farmacologia , Tiazinas/farmacologia
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